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生氰糖苷苦杏仁苷(D-扁桃腈-β-D-葡萄糖苷)是一种新型的DNA聚合酶β抑制剂。

The cyanogenic glucoside, prunasin (D-mandelonitrile-beta-D-glucoside), is a novel inhibitor of DNA polymerase beta.

作者信息

Mizushina Y, Takahashi N, Ogawa A, Tsurugaya K, Koshino H, Takemura M, Yoshida S, Matsukage A, Sugawara F, Sakaguchi K

机构信息

Department of Applied Biological Science, Science University of Tokyo, Noda, Chiba, 278-8510, Japan.

出版信息

J Biochem. 1999 Aug;126(2):430-6. doi: 10.1093/oxfordjournals.jbchem.a022468.

Abstract

A DNA polymerase beta (pol. beta) inhibitor has been isolated independently from two organisms; a red perilla, Perilla frutescens, and a mugwort, Artemisia vulgaris. These molecules were determined by spectroscopic analyses to be the cyanogenic glucoside, D-mandelonitrile-beta-D-glucoside, prunasin. The compound inhibited the activity of rat pol. beta at 150 microM, but did not influence the activities of calf DNA polymerase alpha and plant DNA polymerases, human immunodefficiency virus type 1 reverse transcriptase, calf terminal deoxynucleotidyl transferase, or any prokaryotic DNA polymerases, or DNA and RNA metabolic enzymes examined. The compound dose-dependently inhibited pol. beta activity, the IC(50) value being 98 microM with poly dA/oligo dT(12-18) and dTTP as the DNA template and substrate, respectively. Inhibition of pol. beta by the compound was competitive with the substrate, dTTP. The inhibition was enhanced in the presence of fatty acid, and the IC(50) value decreased to approximately 40 microM. In the presence of C(10)-decanoic acid, the K(i) value for substrate dTTP decreased by 28-fold, suggesting that the fatty acid allowed easier access of the compound to the substrate-binding site.

摘要

一种DNA聚合酶β(pol.β)抑制剂已从两种生物体中独立分离出来,即紫苏(Perilla frutescens)和艾草(Artemisia vulgaris)。通过光谱分析确定这些分子为生氰糖苷D-扁桃腈-β-D-葡萄糖苷(苦杏仁苷)。该化合物在150微摩尔浓度时抑制大鼠pol.β的活性,但不影响小牛DNA聚合酶α、植物DNA聚合酶、人类免疫缺陷病毒1型逆转录酶、小牛末端脱氧核苷酸转移酶或任何所检测的原核DNA聚合酶以及DNA和RNA代谢酶的活性。该化合物剂量依赖性地抑制pol.β活性,以聚dA/寡聚dT(12 - 18)和dTTP分别作为DNA模板和底物时,IC(50)值为98微摩尔。该化合物对pol.β的抑制作用与底物dTTP具有竞争性。在脂肪酸存在的情况下抑制作用增强,IC(50)值降至约40微摩尔。在癸酸存在的情况下,底物dTTP的K(i)值降低了28倍,这表明脂肪酸使该化合物更容易进入底物结合位点。

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